loader
Please Wait
Applying Filters...

Approved Drug Products containing Trifluoperazine Hydrochloride listed in the FDA Orange Book. Original Data : FDA Website

Menu
$ API Ref.Price (USD/KG) : 254Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 4ATHEM

02 1CHARTWELL RX

03 4DURAMED PHARMS BARR

04 6GLAXOSMITHKLINE

05 4IVAX PHARMS

06 4MYLAN

07 1QUAD PHARMS

08 4SANDOZ

09 4WATSON LABS

10 1WOCKHARDT

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Approval Date : 1996-10-25

Application Number : 40153

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

02

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Approval Date : 1996-10-25

Application Number : 40153

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

03

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Approval Date : 1996-10-25

Application Number : 40153

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

04

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 1996-10-25

Application Number : 40153

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

05

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Formnext Forum
Not Confirmed
arrow
arrow
Formnext Forum
Not Confirmed

TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11552

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank